K-number	K894828
Device name	HPI ORTHO SURGEONS' GLOVE
Applicant	Tillotson Rubber Co., Inc.
Product code	KGO
Device class	Class I
Decision date	May 7, 1990
Decision	Substantially Equivalent
Regulation	878.4460

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View the full FDA submission: accessdata.fda.gov

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HPI ORTHO SURGEONS' GLOVE

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